21367009: Autosomal dominant variant form of albumin (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos d'une région de la tête et du cou\Finding of neck region\...
• \Finding of thyroid gland\affection de la glande thyroïde (trouble)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \affection du cou\affection de la glande thyroïde (trouble)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant variant form of albumin
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\affection d'un système corporel\pathologie endocrinologique\affection de la glande thyroïde (trouble)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\affection du cou\affection de la glande thyroïde (trouble)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\trouble métabolique\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
• \Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
35885010	Autosomal dominant variant form of albumin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
750653014	Autosomal dominant variant form of albumin (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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